1960
DOI: 10.1002/cber.19600930719
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Beiträge zur Chemie der Carbinolamine, III. Synthesen und Reaktionsweisen von 2‐[β‐Hydroxy‐äthyl]‐isocarbostyrilen

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1961
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Cited by 32 publications
(3 citation statements)
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“…mum ion (225) is not in equilibrium with its starting ally) derivative (224) or vinyl derivative ( 226), but this ion must be captured by O (or S) before proton loss occurs. 175 The great resistance to H-D exchange at the 2-methyl group indicates the charge is very effectively localized over the two heteroatoms.…”
Section: Methods Of Formationmentioning
confidence: 99%
“…mum ion (225) is not in equilibrium with its starting ally) derivative (224) or vinyl derivative ( 226), but this ion must be captured by O (or S) before proton loss occurs. 175 The great resistance to H-D exchange at the 2-methyl group indicates the charge is very effectively localized over the two heteroatoms.…”
Section: Methods Of Formationmentioning
confidence: 99%
“…Soc., 90, 5303 (1968). (14) These tetrafluoroborates were prepared from the corresponding ortho esters according to the procedure of ref 13.…”
mentioning
confidence: 99%
“…Ethylene Oxide Mediated Conversion of Isoquinolines to Isoquinolones and Oxazolidines. Its Extension to Related Nitrogen Heterocycles1 Received -July 14,1978 Treatment of l-(3-methoxy-2-nitrobenzyl)isoquinoline (lb) with ethylene oxide in acetic acid afforded stable 10b-(3-methoxy-2-nitrobenzyl)oxazolo[2,3-a]isoquinoline (3b). Similarly, 1-cyanoisoquinoline (lc) yielded N-(2hydroxyethyl)-1 -isoquinolone (6a) and /V-(2-acetoxyethyl)-l-isoquinolone (6b).…”
mentioning
confidence: 99%